Canonical Allele Identifier: CA1777411982
Gene: STAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38146894_38146898delinsAAGAT , CM000670.2:g.38146894_38146898delinsAAGAT GRCh38
NC_000008.10:g.38004412_38004416delinsAAGAT , CM000670.1:g.38004412_38004416delinsAAGAT GRCh37
NC_000008.9:g.38123569_38123573delinsAAGAT NCBI36
NG_011827.1:g.9185_9189delinsATCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.307-451_307-447delinsATCTT MANE Select ENSP00000276449.3:n.307-451_307-447delinsATCTT
ENST00000276449.8:c.307-451_307-447delinsATCTT ENSP00000276449.3:n.307-451_307-447delinsATCTT
ENST00000520114.1:n.794-451_794-447delinsATCTT
ENST00000521236.1:c.61-451_61-447delinsATCTT ENSP00000430030.1:n.61-451_61-447delinsATCTT
ENST00000522050.1:c.243-451_243-447delinsATCTT
NM_000349.2:c.307-451_307-447delinsATCTT NP_000340.2:n.307-451_307-447delinsATCTT
XM_006716392.1:c.307-451_307-447delinsATCTT XP_006716455.1:n.307-451_307-447delinsATCTT
NM_000349.3:c.307-451_307-447delinsATCTT MANE Select NP_000340.2:n.307-451_307-447delinsATCTT